Pharma Quality Control Officer

Position Overview:

We are looking for a dedicated and detail-oriented QC Officer to join our office-based Quality Control team. This role is focused on documentation, review, and coordination activities, without involvement in laboratory testing. The QC Officer will play a key role in maintaining the integrity of quality systems and supporting regulatory and quality assurance functions.

Key Responsibilities:

• Document Review & Preparation:
• Prepare and review key quality documents such as:
• ST/MoA (Specifications and Methods of Analysis)
• AMV (Analytical Method Validation documents)
• Finished Product Specifications
• Certificate of Analysis (CoA)
• Stability protocols and reports
• Other documents
• Validation Support:
• Draft and review validation protocols and reports in alignment with applicable guidelines and internal SOPs.
• Quality Standards Oversight:
• Establish and review specifications for finished products and APIs in accordance with regulatory and internal quality standards.
• Regulatory Support:
• Assist the Regulatory Affairs team with documentation for submissions, audits, and query responses.
• Quality System Awareness:
• Apply knowledge of QA principles, including:
• CAPA (Corrective and Preventive Actions)
• Change Control
• Deviation handling and documentation
• Audit Participation:
• Support internal and external audits (regulatory or customer) through documentation readiness and audit coordination.
• Cross-functional Support:
• Provide assistance on any quality-related assignments or projects as directed by QC leadership.

Qualifications & Skills:

• Education: Bachelor's or Master’s degree in Pharmacy, Chemistry, or related field.
• Experience: 2–5 years in a QC documentation or compliance role within the pharmaceutical or healthcare industry.
• Skills Required:
• Strong understanding of GMP, ICH, and regulatory requirements
• Proficient in preparing and reviewing quality documents
• Knowledge of QA concepts such as CAPA and audit management
• Excellent organizational and communication skills
• Attention to detail and commitment to compliance

Work Environment:

• This is a non-laboratory, office-based position.
• Collaboration with QA, Regulatory Affairs, and other departments is essential.
• Some participation in plant visits or audits may be required, but routine lab work is not part of this role.

Job Types: Full-time, Permanent

Pay: ₹20,000.00 - ₹35,000.00 per month

Schedule:

• Day shift

Ability to commute/relocate:

• Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (Required)

Education:

• Bachelor's (Required)

Experience:

• Quality control: 2 years (Required)
• Pharmaceutical manufacturing : 1 year (Preferred)

Willingness to travel:

• 25% (Preferred)

Work Location: In person

Application Deadline: 18/07/2025